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H P Zenner

Showing results (221-230 of 255) with videos related to

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International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
Audiology & Neuro-Otology|April 3, 1999
Dynamics of middle ear prostheses - simulations and measurementsA Eiber, H G Freitag, C Burkhardt, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
HNO|December 10, 1998
[First implantation of a totally implantable electronic hearing aid in patients with inner ear hearing loss]H P Zenner, M M Maassen, P K Plinkert, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, et al.
HNO|December 10, 1998
[A totally implantable hearing aid for inner ear deafness: TICA LZ 3001]H Leysieffer, J W Baumann, R Mayer, et al.
FEBS Letters|December 19, 1994
A structural determinant of differential sensitivity of cloned inward rectifier K+ channels to intracellular spermineB Fakler, U Brändle, C Bond, et al.
Pageof 26

Showing results (221-230 of 255) with videos related to

Sort By:
Pageof 26
International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
Audiology & Neuro-Otology|April 3, 1999
Dynamics of middle ear prostheses - simulations and measurementsA Eiber, H G Freitag, C Burkhardt, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
HNO|March 19, 2004
[Waardenburg syndrome. A heterogenic disorder with variable penetrance]F Apaydin, M Bereketoglu, O Turan, et al.
HNO|December 10, 1998
[First implantation of a totally implantable electronic hearing aid in patients with inner ear hearing loss]H P Zenner, M M Maassen, P K Plinkert, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|April 20, 1999
Comparative study of visual, auditory, and olfactory function in Usher syndromeM Seeliger, M Pfister, K Gendo, et al.
HNO|December 10, 1998
[A totally implantable hearing aid for inner ear deafness: TICA LZ 3001]H Leysieffer, J W Baumann, R Mayer, et al.
FEBS Letters|December 19, 1994
A structural determinant of differential sensitivity of cloned inward rectifier K+ channels to intracellular spermineB Fakler, U Brändle, C Bond, et al.
Pageof 26